Canonical Allele Identifier: CA2595736961
Gene: LINC00951 HGNC NCBI

Linked Data

dbSNP Id: rs2113771105
gnomAD v3: 6-40354224-C-T
gnomAD v4: 6-40354224-C-T
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Genomic Alleles

HGVS Genome Assembly
NC_000006.12:g.40354224C>T , CM000668.2:g.40354224C>T GRCh38
NC_000006.11:g.40321963C>T , CM000668.1:g.40321963C>T GRCh37
NC_000006.10:g.40429941C>T NCBI36

Transcript Alleles

HGVS Amino-acid Change
NR_038887.1:n.1783G>A
Search 100 bp 5'
Search 100 bp 3'